French Speak Complaints Vigilance Consultant Medical Device

4 days left

Highly Competitive
Oct 04, 2016
Nov 01, 2016
Owen Bach
Result Type
Position Type
Full Time

Our client is a medical device company based in the South of France. They are currently searching for a Complaints Handling consultant to join them on remediation project that will last for the next 6 to 18 months.

The Complaints Handling Consultant will be responsible for coordination of market reports (complaints), review and remediation action of complaint files according to defined protocols and coordination of all complaint processes.

To be successful in this role you must be fluent in both English and French. You will have a proven track record of complaints handling within the medical device sector. You should have prior experience of filing MDVs and MDRs and ideally have experience of running FSCA (field safety correcting action). Experience of IEC 60601 or IEC 62304 would be desirable.

This is an exciting opportunity to join a well-known company in a project in a desirable location, for a project that will last between 6 and 18 months.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Owen Back on 0203 8261 330 or upload your CV on our website A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.


KEY WORDS: Complaints Handling, investigation, post-market vigilance, FDA, Quality Assurance, Quality Engineer, assurance qualité, Ingénieur Qualité, medical device, ISO 13485, CAPA, Validation, surveillance, QA, corrective action, preventative action, remediation, remedial, project

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